TP53, tumor protein p53, 7157

N. diseases: 84; N. variants: 390
Disease: MYELODYSPLASTIC SYNDROME ×
Source: CLINVAR ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11540652
rs11540652
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		T 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11540652
rs11540652
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		G 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs11540652
rs11540652
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121912651
rs121912651
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		C 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016
dbSNP: rs121912651
rs121912651
Entrez Id: 7157
Gene Symbol: TP53
TP53
CUI: C3463824
Disease:
MYELODYSPLASTIC SYNDROME 		A 0.700 GeneticVariation CLINVAR Identifying recurrent mutations in cancer reveals widespread lineage diversity and mutational specificity. 26619011 2016